Preclinical Safety/Toxicology and Strategic Regulatory Consulting for biotech startups with focus from preclinic to first-in-human trial.
Products, services, technology
Creating Preclinical Development Plan, Developing preclinical study plans/designs, Interacting with Regulatory Authorities and CROs, CRO selection and Study Monitor, Reviewing toxicology reports, Support in preparation of the preclinical safety sections for regulatory documentation.
- +41 76 324 82 50
- lisa.fischer@fischerpreclintox.ch
- Lisa Fischer
Some insights
My company try to close the gap between bench and bedside in supporting biotech start-ups and SMEs to bring faster their innovative treatments to patients.
As I am my own boss now, I am able to decide actively for the support of female founders and hopefully to grow up the number of female founders in future.
Founders of biotech start-ups and SMEs